Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Wound tenderness (finding) | 225944008 | |
| Angulation osteotomy of diaphysis and internal fixation (procedure) | 448052002 | |
| Entire cartilage of Eustachian tube (body structure) | 362565000 | |
| Temporal resolution (observable entity) | 250898009 | |
| Pecten species diagnostic allergen extract (product) | 411749004 | |
| Primary adenocarcinoma of middle lobe of right lung (disorder) | 1078951000119101 | |
| Ferri-hemoglobin (substance) | 27980006 | |
| 12000 (qualifier value) | 732476000 | |
| Pseudoalteromonas undina (organism) | 438081003 | |
| Method of patient identification (attribute) | 405683004 | |
| Reagin reaction, function (observable entity) | 124921002 | |
| Mansonia uniformis (organism) | 38878008 | |
| Primary cystadenocarcinoma of oropharynx (disorder) | 707589002 | |
| Cochlear electrode array introducer (physical object) | 714065004 | |
| Mitral valve prolapse syndrome (disorder) | 8074002 | |
| Hemoglobin Bart's hydrops syndrome (disorder) | 5300004 | [A severe form of alpha-thalassemia that is mostly lethal, and associated with severe long-term outcome and lifelong transfusions in survivors. It is characterized by fetal onset of generalized edema, pleural and pericardial effusions, and severe hypochromic anemia. Caused by deletion or inactivation of all four alpha-globin alleles leading to a severe deficiency in alpha-globin chains of Hb, and to the production of gamma-4 tetramers (Hb Bart's) during fetal life, and beta-4 tetramers (HbH) postnatally. Hb Bart's and HbH have increased oxygen affinity resulting in ineffective tissue oxygen delivery. The disease is mostly the result of combined, biallelic deletions in the HBA1 and HBA2 genes (16p13.3). The pattern of inheritance is autosomal recessive., A severe form of alpha-thalassaemia that is mostly lethal, and associated with severe long-term outcome and lifelong transfusions in survivors. It is characterized by fetal onset of generalised oedema, pleural and pericardial effusions, and severe hypochromic anaemia. Caused by deletion or inactivation of all four alpha-globin alleles leading to a severe deficiency in alpha-globin chains of Hb, and to the production of gamma-4 tetramers (Hb Bart's) during fetal life, and beta-4 tetramers (HbH) postnatally. Hb Bart's and HbH have increased oxygen affinity resulting in ineffective tissue oxygen delivery. The disease is mostly the result of combined, biallelic deletions in the HBA1 and HBA2 genes (16p13.3). The pattern of inheritance is autosomal recessive.] |
| Fetal anemia (disorder) | 462166006 | |
| Effective therapeutic regimen management (finding) | 129830006 | |
| Blood sampling from hemodialysis circuit (procedure) | 243777005 | |
| Pyroglutamyl-peptidase I inhibitor (disposition) | 784012003 |